An Easy and Efficient Synthesis of 3-Nitrochromans.
β Scribed by Ching-Fa Yao; Yeong-Jiunn Jang; Ming-Chung Yan
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 139 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
An Easy and Efficient Synthesis of 3-Nitrochromans. -The reaction of nitro olefins (II) with (I) in the presence of DABCO generates 3-nitrochromans (III) with a high stereoselectivity. Interestingly, the sam nitrochroman is formed from both the (E)-nitroolefin and from the corresponding (Z)-isomer indicating a stepwise mechanism. -
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract 3β²βAminoβ3β²βdeoxyguanosine was synthesized from guanosine in eight steps and 58% overall yield. The 2β²,3β²βdiol of 5β²β__O__β[(__tert__βbutyl)diphenylsilyl]β2β__N__β[(dimethylamino)methylidene]guanosine was reacted with __Ξ±__βacetoxyisobutyryl bromide and treated with 0.5n NH~3~ in MeOH t
2,6-Dibromopyridine N-oxide and 4-nitro-2,6-dibromopyridine N-oxide were treated with tributyl(pyridin-2-yl)stannane under the conditions of the Stille coupling reaction. Derivatives of 2,2Π-bipyridine 1-oxides as well as 2,2Π:6Π,2ΠΠ-terpyridine 1Π-oxides were synthesised. Oxidation of 2,2Π:6Π,2ΠΠ-t